Balcı, B., Gerçeker, F. Ö., Aksoy, S., Sennaroğlu, G., Kalay, E., Sennaroğlu, L., & Dinçer, P. (2005). Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea region in Turkey. The Turkish Journal of Pediatrics, 47(3), 213-221. https://doi.org/10.24953/turkjpediatr.2005.2717